Role of centers with different patient volumes in the management of rhabdomyosarcoma. An analysis by the Italian Pediatric Soft Tissue Sarcoma Committee

Procedure The survival of children with rhabdomyosarcoma (RMS) has gradually improved as a result of the adoption of multidisciplinary treatments. Dedicated skills and facilities are indispensable and more readily available at reference centers. In this study, we examined the role of centers’ experi...

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Published inPediatric blood & cancer Vol. 68; no. 12; pp. e29234 - n/a
Main Authors Bisogno, Gianni, Congiu, Giovanna, Affinita, Maria Carmen, Milano, Giuseppe Maria, Zanetti, Ilaria, Coppadoro, Beatrice, Manzitti, Carla, Basso, Eleonora, Tamburini, Angela, Melchionda, Fraia, Cellini, Monica, Pericoli, Roberta, D'Angelo, Paolo, Cataldo, Andrea Di, De Leonardis, Francesco, Rabusin, Marco, De Corti, Federica, Zin, Angelica, Alaggio, Rita, Scarzello, Giovanni, Ferrari, Andrea
Format Journal Article
LanguageEnglish
Published United States Wiley Subscription Services, Inc 01.12.2021
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Abstract Procedure The survival of children with rhabdomyosarcoma (RMS) has gradually improved as a result of the adoption of multidisciplinary treatments. Dedicated skills and facilities are indispensable and more readily available at reference centers. In this study, we examined the role of centers’ experience (based on the number of patients treated) in their management of patients with RMS. Methods We analyzed 342 patients with localized RMS enrolled in the European RMS 2005 protocol from October 2005 to December 2016 at 31 Italian centers that are part of the Soft Tissue Sarcoma Committee (STSC). We grouped the centers by the number of patients each one enrolled (Group 1: >40; Group 2: <40 and >10; and Group 3: <10), and compared a number of indicators to assess the appropriateness of patients’ diagnostic workup and treatment and their survival. Results Overall, 74.6% of patients were treated at 10 centers, and only three of them classifiable as high‐volume centers. Only minor differences emerged between the three patient groups in terms of diagnostic investigations and treatment modalities. Survival was similar in the three groups. Approximately, one in four children treated at the centers in Groups 2 and 3 traveled to another center for surgery or radiotherapy. Conclusion Patients treated at STSC centers with different amounts of experience had similar results in terms of survival. This is attributable to all centers in the network adhering to protocol recommendations and receiving the STSC's support on diagnostics and multidisciplinary treatments for RMS.
AbstractList PROCEDUREThe survival of children with rhabdomyosarcoma (RMS) has gradually improved as a result of the adoption of multidisciplinary treatments. Dedicated skills and facilities are indispensable and more readily available at reference centers. In this study, we examined the role of centers' experience (based on the number of patients treated) in their management of patients with RMS. METHODSWe analyzed 342 patients with localized RMS enrolled in the European RMS 2005 protocol from October 2005 to December 2016 at 31 Italian centers that are part of the Soft Tissue Sarcoma Committee (STSC). We grouped the centers by the number of patients each one enrolled (Group 1: >40; Group 2: <40 and >10; and Group 3: <10), and compared a number of indicators to assess the appropriateness of patients' diagnostic workup and treatment and their survival. RESULTSOverall, 74.6% of patients were treated at 10 centers, and only three of them classifiable as high-volume centers. Only minor differences emerged between the three patient groups in terms of diagnostic investigations and treatment modalities. Survival was similar in the three groups. Approximately, one in four children treated at the centers in Groups 2 and 3 traveled to another center for surgery or radiotherapy. CONCLUSIONPatients treated at STSC centers with different amounts of experience had similar results in terms of survival. This is attributable to all centers in the network adhering to protocol recommendations and receiving the STSC's support on diagnostics and multidisciplinary treatments for RMS.
The survival of children with rhabdomyosarcoma (RMS) has gradually improved as a result of the adoption of multidisciplinary treatments. Dedicated skills and facilities are indispensable and more readily available at reference centers. In this study, we examined the role of centers' experience (based on the number of patients treated) in their management of patients with RMS. We analyzed 342 patients with localized RMS enrolled in the European RMS 2005 protocol from October 2005 to December 2016 at 31 Italian centers that are part of the Soft Tissue Sarcoma Committee (STSC). We grouped the centers by the number of patients each one enrolled (Group 1: >40; Group 2: <40 and >10; and Group 3: <10), and compared a number of indicators to assess the appropriateness of patients' diagnostic workup and treatment and their survival. Overall, 74.6% of patients were treated at 10 centers, and only three of them classifiable as high-volume centers. Only minor differences emerged between the three patient groups in terms of diagnostic investigations and treatment modalities. Survival was similar in the three groups. Approximately, one in four children treated at the centers in Groups 2 and 3 traveled to another center for surgery or radiotherapy. Patients treated at STSC centers with different amounts of experience had similar results in terms of survival. This is attributable to all centers in the network adhering to protocol recommendations and receiving the STSC's support on diagnostics and multidisciplinary treatments for RMS.
Abstract Procedure The survival of children with rhabdomyosarcoma (RMS) has gradually improved as a result of the adoption of multidisciplinary treatments. Dedicated skills and facilities are indispensable and more readily available at reference centers. In this study, we examined the role of centers’ experience (based on the number of patients treated) in their management of patients with RMS. Methods We analyzed 342 patients with localized RMS enrolled in the European RMS 2005 protocol from October 2005 to December 2016 at 31 Italian centers that are part of the Soft Tissue Sarcoma Committee (STSC). We grouped the centers by the number of patients each one enrolled (Group 1: >40; Group 2: <40 and >10; and Group 3: <10), and compared a number of indicators to assess the appropriateness of patients’ diagnostic workup and treatment and their survival. Results Overall, 74.6% of patients were treated at 10 centers, and only three of them classifiable as high‐volume centers. Only minor differences emerged between the three patient groups in terms of diagnostic investigations and treatment modalities. Survival was similar in the three groups. Approximately, one in four children treated at the centers in Groups 2 and 3 traveled to another center for surgery or radiotherapy. Conclusion Patients treated at STSC centers with different amounts of experience had similar results in terms of survival. This is attributable to all centers in the network adhering to protocol recommendations and receiving the STSC's support on diagnostics and multidisciplinary treatments for RMS.
Procedure The survival of children with rhabdomyosarcoma (RMS) has gradually improved as a result of the adoption of multidisciplinary treatments. Dedicated skills and facilities are indispensable and more readily available at reference centers. In this study, we examined the role of centers’ experience (based on the number of patients treated) in their management of patients with RMS. Methods We analyzed 342 patients with localized RMS enrolled in the European RMS 2005 protocol from October 2005 to December 2016 at 31 Italian centers that are part of the Soft Tissue Sarcoma Committee (STSC). We grouped the centers by the number of patients each one enrolled (Group 1: >40; Group 2: <40 and >10; and Group 3: <10), and compared a number of indicators to assess the appropriateness of patients’ diagnostic workup and treatment and their survival. Results Overall, 74.6% of patients were treated at 10 centers, and only three of them classifiable as high‐volume centers. Only minor differences emerged between the three patient groups in terms of diagnostic investigations and treatment modalities. Survival was similar in the three groups. Approximately, one in four children treated at the centers in Groups 2 and 3 traveled to another center for surgery or radiotherapy. Conclusion Patients treated at STSC centers with different amounts of experience had similar results in terms of survival. This is attributable to all centers in the network adhering to protocol recommendations and receiving the STSC's support on diagnostics and multidisciplinary treatments for RMS.
Author Bisogno, Gianni
Affinita, Maria Carmen
Ferrari, Andrea
Coppadoro, Beatrice
Zin, Angelica
Milano, Giuseppe Maria
De Leonardis, Francesco
Manzitti, Carla
D'Angelo, Paolo
Cataldo, Andrea Di
Congiu, Giovanna
Cellini, Monica
Basso, Eleonora
Pericoli, Roberta
Alaggio, Rita
Melchionda, Fraia
Scarzello, Giovanni
Zanetti, Ilaria
Tamburini, Angela
De Corti, Federica
Rabusin, Marco
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  organization: A. Meyer Children's Hospital
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  givenname: Andrea Di
  orcidid: 0000-0002-4509-3066
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  organization: Veneto Institute of Oncology, IRCCS
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  givenname: Andrea
  orcidid: 0000-0002-4724-0517
  surname: Ferrari
  fullname: Ferrari, Andrea
  organization: Fondazione IRCCS Istituto Nazionale Tumori
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Issue 12
Keywords rhabdomyosarcoma
centers’ experience
multidisciplinary treatment
network
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Snippet Procedure The survival of children with rhabdomyosarcoma (RMS) has gradually improved as a result of the adoption of multidisciplinary treatments. Dedicated...
The survival of children with rhabdomyosarcoma (RMS) has gradually improved as a result of the adoption of multidisciplinary treatments. Dedicated skills and...
Abstract Procedure The survival of children with rhabdomyosarcoma (RMS) has gradually improved as a result of the adoption of multidisciplinary treatments....
ProcedureThe survival of children with rhabdomyosarcoma (RMS) has gradually improved as a result of the adoption of multidisciplinary treatments. Dedicated...
PROCEDUREThe survival of children with rhabdomyosarcoma (RMS) has gradually improved as a result of the adoption of multidisciplinary treatments. Dedicated...
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StartPage e29234
SubjectTerms centers’ experience
Child
Children
Hematology
Humans
Italy
multidisciplinary treatment
network
Oncology
Patients
Pediatrics
Radiation therapy
Rhabdomyosarcoma
Rhabdomyosarcoma - surgery
Rhabdomyosarcoma, Embryonal
Sarcoma
Soft Tissue Neoplasms - therapy
Soft tissue sarcoma
Survival
Title Role of centers with different patient volumes in the management of rhabdomyosarcoma. An analysis by the Italian Pediatric Soft Tissue Sarcoma Committee
URI https://onlinelibrary.wiley.com/doi/abs/10.1002%2Fpbc.29234
https://www.ncbi.nlm.nih.gov/pubmed/34260145
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Volume 68
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